Composition for heart disease, its active ingredients, method to prepare same and uses thereof

ABSTRACT

This invention provides a composition for heart disease comprising extracts from raw herbs of 80.0-97.0% Radix Salviae Miltorrhizae, 1.0-19.0% Panax Notoginseng and 0.1-1.0% Borneol and its active ingredients. This invention also provides a method for preparing said composition and the active ingredients of the composition. Finally, this invention provides various uses of said compositions and the active ingredients.

The application disclosed herein claims benefit of U.S. Ser. No. 60/491,466, Filed Jul. 31, 2003, the content of which are hereby incorporated in its entirety by reference into this application.

Throughout this application, various publications are referenced and full citations for these publications may be found in the text where they are referenced. Disclosures of these publications in their entireties are hereby incorporated by reference into this application to more fully describe the state of the art to which this invention pertains.

BACKGROUND OF THE INVENTION

Heart disease includes a number of conditions affecting the structure or function of the heart. They can include: coronary artery disease, including heart attack, abnormal heart rhythms, heart failure, heart valve disease, congenital heart disease, heart muscle disease or cardiomyopathy, and pericardial disease.

Heart disease is the leading cause of death for both men and women in the United States. Treatment of heart disease depends on the type of disease as well as many additional factors. Coronary artery disease is treated with: medications such as aspirin; beta-blockers; nitroglycerin tablets, sprays, and patches; calcium channel blockers; thrombolytic therapy; and surgeries such as coronary angioplasty and coronary bypass operations.

The number of patients with cardiovascular or cerebrovascular disease increases along with higher living standards (better food supply), the worldwide aging problem, and young adults' involvement. It has become the second-most-common disease worldwide threatening the health of human beings.

Angina pectoris is caused by insufficient blood and oxygen supply to the heart. The main clinical symptom is chest pain. It is caused by atherosclerosis or spasms of the coronary artery in about 90% of angina pectoris patients.

The major treatments for angina pectoris are vessel dilation, lowering of blood viscosity, anti-aggregation of platelets and anti-coagulation. The traditional medicines used are nitrates, beta-adrenoceptor blocking drugs and calcium-channel blocking drugs. However, all these drugs have many side effects which make them unsuitable for long-term use. For example, some patients experience a swelling sensation in their heads, rapid heartbeat and even lapse into coma after taking glyceryl trinitrate.

This invention involves a medication which can prevent and cure coronary heart disease with angina pectoris, the methods of manufacture and other usages of the medication. The medication, Dan Shen Pill (DSP), is made from a variety of Chinese herbs using a series of standard procedures.

DSP is an improvement on Dan Shen Tablet (DST) (recorded in Pharmacopoeia of the People's Republic of China Edition, 1977, 1985, 1995, and 2000), but there are significant differences between DSP and DST, specifically, the proportions in their formulas, manufacturing techniques and their clinical results.

Although there are many Chinese herbal medicines used for treating angina pectoris, fewer people use them nowadays. DST or capsules are still being sold in the market, but their manufacturing techniques are old, their efficacy is low and there are no quality control standards. DST is taken orally and absorbed in the gastrointestinal tract, where it is absorbed into blood vessels after processing in the liver. The bioavailability is low, and the absorption speed is low, which is not suitable for the emergency treatment of patients with angina pectoris. Accordingly, DSP is superior to DST.

Throughout this application, various publications are referenced and the disclosures of these publications are hereby incorporated by reference into this application in order to more fully describe the state of art as known to the skilled artisan therein as of the date of invention described and claimed herein.

SUMMARY OF THE INVENTION

This invention provides a composition and its active ingredients for treating heart disease. The heart disease includes chronic stable angina pectoris, coronary artery disease (including heart attack), abnormal heart rhythm, heart failure, heart valve disease, congenital heart disease, heart muscle disease (cardiomyopathy), and pericardial disease. This invention also provides a composition comprising extracts from raw herbs of 80.0-97.0% Radix Salviae Miltorrhizae, 1.0-19.0% Panax Notoginseng and 0.1-1.0% Borneol.

This invention provides the above composition wherein the extracts are made from raw herbs of 90.0-97.0% Radix Salviae Miltorrhizae, 2.5-9.6% Panax Notoginseng and 0.2-0.5% Borneol. This invention provides the above composition wherein the extracts are made from raw herbs of 89.8% Radix Salviae Miltorrhizae, 9.6% Panax Notoginseng and 0.5% Borneol.

This invention provides a method comprising steps of: (1) obtaining an appropriate amount of smashed Radix Salviae Miltorrhizae and Panax Notoginseng; (2) extracting the obtained Radix Salviae Miltorrhizae, and Panax Notoginseng in hot aqueous reflux; (3) filtering and combining the extracts to form a combined extract; (4) concentrating the combined extract from step (3) to an appropriate ratio of the volume of the concentrated extract to the weight of the inputted herbal materials to form a concentrated extract; (5) precipitation by organic solvent to form a precipitate; (6) concentrating the supernatant liquid of precipitate resulting from step (5) to form a plaster; (7) mixing the plaster from step (6) with an appropriate amount of Borneol, thereby producing the composition comprising extracts of Radix Salviae Miltorrhizae, Panax Notoginseng and Borneol for heart disease.

The above composition contains Sodium 3′4-dihydroxyphenyllactate, 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

In another embodiment, the above composition further contains methyl tanshinonate, methyl rosmarinate, danshexinkum, lithospermic acid, d-borneol, l-borneol, tanshinone I, tanshinone IIA, tanshinone IIB, tanshinone V, tanshinone VI, isotanshinone, miltirone, dihydrotanshinone, 1-dehydrotanshinone and neocryptotanshinone, Salvianolic acid G and Salvianolic acid I, lithospermic acid B, ethyl lithospermate, dimethyl lithospermate, monomethyl lithospermate, ginsenoside Rd, ginsenoside Rg2, ginsenoside Rg3, ginsenoside Rh1 and ginsenoside Rh2, notoginsenoside R2, notoginsenoside R3, notoginsenoside R4, notoginsenoside R6, and notoginsenoside R7.

This invention also provides a pill composition capable of treating chronic stable angina pectoris comprising about 0.14 to about 0.18 mg 3′4-dihydroxyphenyllactate per pill, about 6.50 to about 40.50 mg Sanchinoside R1 per pill and about 25.60 to about 86.20 mg Ginsenoside Rg1 per pill.

This invention provides a composition for the treatment of cardiovascular and cerebrovascular disease comprising active ingredients extracted from Salvia miltiorrhiza Beg., Panax notoginseng or Ginseng, and Dryobalanops aromatica Geartu.F. or Cinnammon camphor or synthetic borneol. The active ingredient extracted from Salvia miltiorrhiza Beg. contains one or more ingredients selected from tanshinone, salvianolic acid, methyl tanshinonate, rosmarinic acid, methyl rosmarinate, danshexinkum, protocatechualdehyde, Sodium 3′4-dihydroxyphenyllactate, and lithospermic acid. The ingredient extracted from Panax notoginseng or Ginseng contains one or more ingredients selected from notoginsenoside and ginsenoside. The ingredient extracted from Dryobalanops aromatica Geartu.F. or Cinnammon camphor. contains d-borneol or l-borneol or both of them.

The said tanshinone includes tanshinone I, tanshinone IIA, tanshinone IIB, tanshinone V, tanshinone VI, isotanshinone, miltirone, dihydrotanshinone, 1-dehydrotanshinone, and neocryptotanshinone. The said salvianolic acid includes Salvianolic acid A, Salvianolic acid B, Salvianolic acid C, Salvianolic acid D, Salvianolic acid E, Salvianolic acid G, and Salvianolic acid I. The said lithospermic acid includes lithospermic acid B, ethyl lithospermate, dimethyl lithospermate, and monomethyl lithospermate. The said ginsenoside includes ginsenoside Rb1, ginsenoside Rd, ginsenoside Re, ginsenoside Rg1, ginsenoside Rg2, ginsenoside Rg3, ginsenoside Rh1, and ginsenoside Rh2. The said notoginsenoside includes notoginsenoside R1, notoginsenoside R2, notoginsenoside-R3, notoginsenoside R4, notoginsenoside R6, and notoginsenoside R7.

This invention provides the above composition comprising Magnesium Salvianolate B or 3′4-dihydroxyphenyllactate extracted from the Salvia miltiorrhiza Beg., Ginsenoside Rb₁ extracted from the Panax notoginseng or Ginseng, and d-Borneol extracted from the Dryobalanops aromatica Geartu.F. or Cinnammon camphor. In an embodiment, the composition comprises 10-80 mg of Magnesium Salvianolate B, 10-50 mg of Ginsenoside Rb₁ and 5-30 mg of Borneol. In a further embodiment, the composition is characterized by comprising 50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol.

This invention provides the above composition, comprising 5-80 mg of sodium 3′4-dihydroxyphenyllactate, 10-50 mg of Ginsenoside Rb₁ and 5-30 mg of Borneol. In a further embodiment, this invention provides the above composition comprising 20 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol.

This invention provides the above composition further comprising one or more kinds of excipients, such as polyethylene glycol, xylitol, lactobacillus, starch for preparation of dripping pills, wherein the ratio of weight of the above total extracts or above total pure ingredients to the weight of excipient is 1:1-1:4. For example, 50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁, 15 mg of d-Borneol and 265 mg of excipient are contained per ten dripping pills; 20 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol and 265 mg of excipient are contained per ten dripping pills.

The Salvianolate B was extracted by steps of: pulverizing Salvia miltiorrhiza Beg. into a fine powder, and decocting twice with hot water; combining the decoctions, and concentrating under vacuum at about 50° C.; loading the solution from the step (b) into macroporous adsorption resin and, after washing with water, eluting column with 40% ethanol; After recovering the ethanol from solution obtained in the step (c), refining it by Sephadex LH-20 or other gel columns with the similar characteristics, eluting with ethanol and collecting eluant containing Magnesium Salvianolate B; repeating the process of step (d) until the concentration of Magnesium Salvianolate B reaches more than 90%. The purity of concentration of Magnesium Salvianolate B was assayed by HPLC at a detective wavelength of 281 nm.

The Ginsenoside Rb₁ was extracted by steps of: pulverizing Panax notoginseng or Ginseng into fine powder, and decocting with water; or refluxing with 70% ethanol; or percolating with 70% ethanol; recovering solvent from the solution at reduced pressure; loading the solution from the step (b) into macroporous adsorption resin, and after washing with water, eluting column with 40% ethanol; After recovering the ethanol from solution obtained in the step (c), refining it by silica gel column; eluting the column with chloroform, methanol and water in the ratio of 6:3:1, respectively, and collecting eluant; Using TLC for examination of Ginsenoside Rb₁ and recovering the solvent, thereby obtaining Ginsenoside Rb₁.

DETAILED DESCRIPTION OF THE INVENTION

This invention provides a composition for treating heart disease. Heart disease includes chronic stable angina pectoris, coronary artery disease (including heart attack), abnormal heart rhythm, heart failure, heart valve disease, congenital heart disease, heart muscle disease (cardiomyopathy), and pericardial disease.

This invention provides a composition for treatment of heart disease comprising the extract of raw herbs of Radix Salviae Miltorrhizae, Panax Notoginseng and Borneol.

This invention also provides a composition comprising herb extracts from raw herbs of 80.0-97.0% Radix Salviae Miltorrhizae, 1.0-19.0% Panax Notoginseng and 0.1-1.0% Borneol.

This invention provides the above composition wherein the extracts are made from raw herbs of 90.0-97.0% Radix Salviae Miltorrhizae, 2.5-9.6% Panax Notoginseng and 0.2-0.5% Borneol.

This invention provides the above composition wherein the extracts are made from raw herbs of 89.8% Radix Salviae Miltorrhizae, 9.6% Panax Notoginseng and 0.5% Borneol.

This invention provides a preparation method comprising steps of: (1) obtaining an appropriate amount of smashed Radix Salviae Miltorrhizae and Panax Notoginseng; (2) extracting the obtained Radix Salviae Miltorrhizae and Panax Notoginseng in hot aqueous reflux; (3) filtering and combining the extracts to form a combined extract; (4) concentrating the combined extract from step (3) to an appropriate ratio of the volume of the concentrated extract to the weight of the inputted herbal materials to form a concentrated extract; (5) precipitating by organic solvent to form a precipitate; (6) concentrating the supernatant liquid of precipitate resulting from step (5) to form a plaster; (7) mixing the plaster from step (6) with an appropriate amount of Borneol, thereby producing the composition comprising extracts of Radix Salviae Miltorrhizae, Panax Notoginseng and Borneol for heart disease.

In an embodiment, the hot aqueous reflux is at about 60-100° C. In another embodiment, the ratio of the volume of the concentrated extract to the weight of the inputted herbal materials is 1 liter: about 0.7-1.3 kg of herbal material. In a separate embodiment of step (5), ethanol is used for precipitation. In a further embodiment, the concentrated extract from step (5) is added to a final concentration of about 50-85% ethanol. In another embodiment, the plaster is about 1.15-1.45 in relative density.

The above composition contains Sodium 3′4-dihydroxyphenyllactate, 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

In another embodiment, the above composition further contains methyl tanshinonate, methyl rosmarinate, danshexinkum, lithospermic acid, d-borneol, l-borneol, tanshinone I, tanshinone IIA, tanshinone IIB, tanshinone V, tanshinone VI, isotanshinone, miltirone, dihydrotanshinone, 1-dehydrotanshinone and neocryptotanshinone, Salvianolic acid G and Salvianolic acid I, lithospermicacid B, ethyl lithospermate, dimethyl lithospermate, monomethyl lithospermate, ginsenoside Rd, ginsenoside Rg2, ginsenoside Rg3, ginsenoside Rh1 and ginsenoside Rh2, notoginsenoside R2, notoginsenoside R3, notoginsenoside R4, notoginsenoside R6, and notoginsenoside R7.

This invention also provides a pill composition capable of treating chronic stable angina pectoris comprising about 0.14 to about 0.18 mg 3′4-dihydroxyphenyllactate per pill, about 6.50 to about 40.50 mg Sanchinoside R1 per pill and about 25.60 to about 86.20 mg Ginsenoside Rg1 per pill.

This invention provides a composition for treatment of chronic stable angina pectoris, comprising 5-40% water-soluble phenolic acid of Radix Salviae Miltorrhizae, 1-10% water-soluble saponin of Panax Notoginseng and 1-5% of Borneol.

This invention provides the composition comprising 10-30% water-soluble phenolic acid of Radix Salviae Miltorrhizae, 2-6% water-soluble saponin of Panax Notoginseng and 1-3% of Borneol.

This invention provides a composition capable of treating chronic stable angina pectoris and produced eight peaks, as shown in FIG. 1, when subjected to steps of: (a) Dissolving a suitable amount of said composition in internal standard para-aminobenzonic acid solvent; (b) Using Danshensu and Protocatechuic Aldehyde as the standards; (c) Performing the HPLC assay; and (d) Calculating according to the internal standard method.

This invention provides a composition capable of treating chronic stable angina pectoris comprising about 0.14 to about 0.18 mg Danshensu per pill, more than 12.12 μg Sanchinoside R1 per pill and more than 56.26 μg Ginsenoside Rg1 per pill.

This invention provides the above composition produced by steps of: (a) Extracting Radix Salviae Miltorrhizae, Panax Notoginseng separately in hot aqueous reflux and filtering separately; (b) Concentrating filtrates separately; (c) Refining the concentrates separately using resin columns and concentrating, and getting refined water-soluble extract of Radix Salviae Miltorrhizae and refined water-soluble extract of Panax Notoginseng; and (d) Mixing the refined water-soluble extracts from step (c) with an appropriate amount of borneol, thereby producing a composition capable of treating chronic stable angina pectoris.

This invention provides the above composition produced by steps of:

-   (1) extraction of water-soluble components of Panax Notoginseng (a)     diluting herbs with 5-7 times water; (b) extracting water-soluble     components of Panax Notoginseng by boiling in a tank with air     pressure between 0.04-0.06 mPa for 2 hours; (c) repeating extraction     under the same conditions for 1.5 hours; (d) filtering the     extraction with 100-mesh net; (e) refining the filtrate using     macroporous adsorption resin eluting with ethanol; and (f)     concentrating the eluted extracts under decompressed conditions with     the air input to 0.04-0.06 mPa and the vacuum to −0.076˜−0.088 mPa     until the density is 1.33-1.35; -   (2) extraction of water-soluble components of Radix Salviae     Miltorrhizae (a) diluting herbs with 5-7 times water; (b) extracting     water-soluble components of Radix Salviae Miltorrhizae by boiling in     a tank with the air pressure between 0.04-0.06 mPa for 2 hours; (c)     repeating extraction under the same condition for 1.5 hours; (d)     Filtering the extraction with 100-mesh net; (e) concentrating the     filtrates under decompressed conditions with vacuum pressure of     −0.076˜-0.088 mPa until one Kg initial herb becomes one liter; (f)     precipitating the concentrates with ethanol; (g) filtering the     ethanol precipitate solution through 100-mesh net; (h) Concentrating     the filtrates under decompressed conditions with input air pressure     of 0.04-0.06 mPa and vacuum pressure of 0.076˜−0.088 mPa; (i)     refining the concentrates by polyamide chromatography eluting with     ethanol; and (j) concentrating the refined extracts to the density     of 1.33-1.35; -   (3) producing the pill. (a) mixing the extracts of Panax     Notoginseng, the extracts of Radix Salviae Miltorrhizae, synthetic     borneol, and polyethylene glycol 6000 at the ratio of     4.0:20.6:1.9:79.5; (b) melting the mixture; (c) manufacturing the     melted mixture to pills using a dropping machine with the following     characteristics: the temperature of the dropping pot is constantly     89-93° C., the cooling solution is liquid paraffin, of which the     temperature is lower than 8° C., the inner diameter of the dropping     head is 1.8 mm, the outer diameter of the dropping head is 2.4 mm,     the distance between the dropping head and the surface of the     cooling solution is 15 cm; and (d) centrifugation of the pills at     800-1100 rpm for 15 minutes to remove oils.

This invention provides the composition for the treatment of chronic stable angina pectoris comprising Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

The herbal composition comprising the above composition should contain 0.14-0.18 mg 3′4-dihydroxyphenyllactate per pill.

This invention provides a composition for the treatment of heart disease comprising pure active ingredients extracted from Salvia miltiorrhiza Beg., Panax notoginseng or Ginseng, and Dryobalanops aromatica Geartu.F. or Cinnammon camphor or synthetic borneol. The active ingredient extracted from Salvia miltiorrhiza Beg. contains one or more ingredients selected from tanshinone, salvianolic acid, methyl tanshinonate, rosmarinic acid, methyl rosmarinate, danshexinkum, protocatechualdehyde, Sodium 3′4-dihydroxyphenyllactate, and lithospermic acid. The ingredient extracted from Panax notoginseng or Ginseng contains one or more ingredients selected from notoginsenoside and ginsenoside. The ingredient extracted from Dryobalanops aromatica Geartu.F. or Cinnammon camphor. contains d-borneol or l-borneol or both of them.

The said tanshinone includes tanshinone I, tanshinone IIA, tanshinone IIB, tanshinone V, tanshinone VI, isotanshinone, miltirone, dihydrotanshinone, 1-dehydrotanshinone, and neocryptotanshinone. The said salvianolic acid includes Salvianolic acid A, Salvianolic acid B, Salvianolic acid C, Salvianolic acid D, Salvianolic acid E, Salvianolic acid G, and Salvianolic acid I. The said lithospermic acid includes lithospermic acid B, ethyl lithospermate, dimethyl lithospermate, and monomethyl lithospermate. The said ginsenoside includes ginsenoside Rb1, ginsenoside Rd, ginsenoside Re, ginsenoside Rg1, ginsenoside Rg2, ginsenoside Rg3, ginsenoside Rh1, and ginsenoside Rh2. The said notoginsenoside includes notoginsenoside R1, notoginsenoside R2, notoginsenoside-R3, notoginsenoside R4, notoginsenoside R6, and notoginsenoside R7.

This invention provides the above composition comprising Magnesium Salvianolate B or 3′4-dihydroxyphenyllactate extracted from the Salvia miltiorrhiza Beg., Ginsenoside Rb₁ extracted from the Panax notoginseng or Ginseng, and d-Borneol extracted from the Dryobalanops aromatica Geartu.F. or Cinnammon camphor. In an embodiment, the composition comprises 10-80 mg of Magnesium Salvianolate B, 10-50 mg of Ginsenoside Rb₁ and 5-30 mg of Borneol. In a further embodiment, the composition is characterized by comprising 50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol.

This invention provides the above composition, comprising 5-80 mg of sodium 3′4-dihydroxyphenyllactate, 10-50 mg of Ginsenoside Rb₁ and 5-30 mg of Borneol. In a further embodiment, this invention provides the above composition comprising 20 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol.

This invention provides the above composition further comprising one or more kinds of excipients, such as polyethylene glycol, xylitol, lactobacillus, and starch for preparation of dripping pills, wherein the ratio of weight of the above total extracts or above total pure ingredients to the weight of excipient is 1:1-1:4. For example, 50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁, 15 mg of d-Borneol and 265 mg of excipient are contained per ten dripping pills; 20 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol and 265 mg of excipient are contained per ten dripping pills.

The Salvianolate B was extracted by steps of: pulverizing Salvia miltiorrhiza Beg. into a fine powder, and decocting twice with hot water; Combining the decoctions, and concentrating under vacuum at about 50° C.; loading the solution from step (b) into macroporous adsorption resin and, after washing with water, eluting column with 40% ethanol; After recovering the ethanol from the solution obtained in step (c), refining it by Sephadex LH-20 or other gel columns with similar characteristics, eluting with ethanol and collecting eluant containing Magnesium Salvianolate B; repeating the process of step (d) until the concentration of Magnesium Salvianolate B reaches more than 90%. The purity of concentration of Magnesium Salvianolate B was assayed by HPLC at a detective wavelength of 281 nm.

The Ginsenoside Rb₁ was extracted by steps of: Pulverizing Panax notoginseng or Ginseng into fine powder, and decocting with water; or refluxing with 70% ethanol; or percolating with 70% ethanol; recovering solvent from the solution at reduced pressure; loading the solution from step (b) into macroporous adsorption resin and, after washing with water, eluting column with 40% ethanol; After recovering the ethanol from the solution obtained in the step (c), refining it by silica gel column; Eluting the column with chloroform, methanol and water in the ratio of 6:3:1, respectively, and collecting eluant; Using TLC for examination of Ginsenoside Rb₁ and recovering the solvent, thereby obtaining Ginsenoside Rb₁.

This invention provides the above composition, wherein d-Borneol was extracted from the trunk of Dryobalanops aromatica Geartu.F. or the leaves of Cinnammon camphor. by means of vapor distillation or supercritical carbon dioxide extraction. In another embodiment, the Borneol is synthetic.

This invention also provides the above compositions, or its ingredients, formulated in a dropping pellet, pill, capsule, granule, tablet, suspension, injection, syrup, tincture, powder, tea, topical solution, nebula, suppository microcapsule, or other pharmaceutically acceptable form.

In other words, this invention provides a pharmaceutical composition comprising the composition or its ingredients described herein and a pharmaceutically acceptable carrier. As known in the art, pharmaceutically acceptable carriers include, but are not limited to, 0.01-0.1M and preferably 0.05M phosphate buffer or 0.8% saline. Additionally, such pharmaceutically acceptable carriers may be aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, lactated Ringer's, or fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers, such as those based on Ringer's dextrose, and the like. Preservatives and other additives may also be present, for example, antimicrobials, antioxidants, chelating agents, inert gases and the like.

This invention provides compositions, or its ingredients capable of increasing blood volume in the coronary artery, relaxing the smooth muscles of blood vessels, improving peripheral circulation, raising the oxygen content in veins, or significantly improving the acute myocardial ischemia or myocardial infarction, protecting the cells from damage by hypoxia or anoxia, protecting cells suffering from myocardial ischemia, improving micro-circulation, preventing arrhythmia, platelet aggregation and thrombosis, dissolving fibrin, lowering blood viscosity, adjusting blood cholesterol or preventing atherosclerosis, raising tolerance to hypoxia or anoxia, preventing the oxidation of lipoprotein or removing the harmful free radicals, lowering plasma ET content, significantly improving liver, kidney and pancreas function, preventing the occurrence or development of blood vessel or nerve diseases, enhancing the immune system, regulating vascular nerve balance.

This invention provides the above compositions and/or its ingredients, capable of preventing and treating cardiovascular and cerebrovascular disease, kidney disease, liver disease, pneumonia, lung or heart disease, pancreatitis, diabetes, vertebral disease, optic vessels disease, optic nerve disease, eccentric headache, chronic stomachitis, dizziness, bone disease, altitude sickness, common diseases of the elderly, treating stable angina pectoris, unstable angina pectoris, angina pectoris of the aged, non-symptomatic myocardial ischemia, different types of coronary heart disease or angina pectoris disease, treating arrhythmia, enlargement of the left ventricle, myocarditis, myocardial infarction or cerebral infraction, treating hyperlipidaemia, high blood viscosity syndrome or high blood pressure, treating diseases caused by micro-circulation disorder, treating stroke, cerebral infarction, cerebral bleeding and other cerebral diseases, treating hepatitis B, chronic liver fibrosis, liver fibrosis, active liver cirrosis, liver cirrosis in the remission period during recovery and other related diseases, treating kidney syndrome and its conjunctive diseases, treating diabetes or its conjunctive diseases, treating cyanosis-type optic vessel diseases, such as venal blockage in the retina, central optic artery blockage in the retina, high blood pressure optic atherosclerosis in the retina, diabetic retinopathy, cento-neuropathy, cento-osmotic neuropathy, ischemic neuropathy, optic neuritis or optic nervous dystrophy, treating dizziness caused by cerebral-arterial ischemia, Meniere's disease, coronary heart disease, treating detrimental death of epicondylus medialis, femoral end necrosis, twisted joints, ligament damage, fractures and proliferation of bone cells, treating bronchitis in children, treating hypoxia or anoxia, and treating Alzheimer's Disease.

This invention provides a dropping machine for manufacturing a small-sized medicament comprising any one of the above described compositions, which can be readily dissolved thus readily delivered to organs, comprising the parts of: (a) Dropping pot in which the temperature of the liquid is 60-100° C.; (b) Apparatus which holds liquid paraffin cooling solution of which the temperature is lower than 8° C.; and (c) Dropping head with 1.8 mm inner diameter and 2.35 mm outer diameter which is distanced from the surface of the cooling solution by approximately 15 cm, said dropping head allowing a dropping speed of over 30 pellets per minute.

This invention provides a method of determining the active fractions (ingredients) of any one of the above compositions which are capable of treating and preventing heart diseases, wherein said method comprising the steps of: (a) fractionating pharmaceutical compositions by high performance liquid chromatography (HPLC); (b) comparing the retention time of the fractions of pharmaceutical compositions with the retention time of saponin R1, saponin Rg1, and saponin Re; and (c) determining if pharmaceutical compositions contain fractions of which retention time is equivalent to the retention time of saponin R1, saponin Rg1 and saponin Re.

This invention provides a method of determining the active fractions (ingredients) of any one of the above compositions which are capable of treating and preventing heart disease, comprising the steps of: (a) Fractionating a pharmaceutical composition by thin layer chromatography (TLC); (b) Comparing the position and color of the fractions of pharmaceutical compositions with the position and color of 3,4-dihydroxyphenyl lactic acid and Protocatechuic Aldehyde; and (c) Determining if pharmaceutical compositions contain the fractions with position and color equivalent to the position and color of 3,4-dihydroxyphenyl lactic acid and Protocatechuic Aldehyde.

The invention also provides a method of treatment using the above compositions and its active ingredients for treating a specific disease. Effective amounts of the composition may be determined and administered to a subject suffering from said disease.

The subject invention further provides a method of treating a subject having a disorder, which comprises administering to the subject a therapeutically effective amount of the above composition and its active ingredients to thereby treat the subject. The subject includes a human and other mammals.

The administration of the composition and its active ingredients may be effected or performed using any of the various methods known to those skilled in the art. The route of administration includes but is not limited to administering intravenously, intramuscularly, intraperitoneally, and subcutaneously.

The therapeutically effective amount of the above compositions may be determined by methods well known to those skilled in the art.

Animal Research

1. The Effects of DSP on Dogs with Myocardial Ischemia and Myocardial Infarction

Based on changes in myocardial oxygen consumption and biochemical standards, pharmaceutical effects DSP on curing coronary heart disease were investigated. DSP can significantly improve myocardial ischemia and myocardial infarction, raise the blood oxygen level of venous sinuses, inhibit the release of CK and LDH caused by damage to cardiac muscles, lower the activity of blood serum CK and LDH, suppress the activity of blood vessel substances, ET and TXB2, and raise the 6-Keto-PGF1/TXB2 ratio.

2. The Protection of Myocardial Ischemical Reperfusion Injury from Hypoxia in Rats

This research stresses the effects of DSP in myocardial ischemical reperfusion injury from hypoxia in rats, especially on the apoptosis of myocardial cells. Results: Myocardial infarction did not occur after 7 hrs of sham operation. Myocardial hypoxia occurred for 1 hr and myocardial infarction occurred sharply after reperfusing for 6 hrs. DSP can reduce the M-IR area and increase the effects with increasing dosage.

3. Propagation of Myocardial Hypoxia in Mice and Effects of Fas/FasL Proteins Under Deoxygenation and Deoxygenation/Re-oxygenation Conditions

Fas gene is an apoptosis-stimulating gene. Its expressed protein product, Fas antigen, is a cell membrane protein. Recently, it was discovered, in experiments on propagation of myocardial hypoxia, that there is a close relationship between the expressed mRNA of Fas gene and myocardial apoptosis. FasL is the ligand of Fas. It is on the surface of transmembrane proteins, which is homologous to the TNF. It can bind to the receptor Fas on the surface of the cell and give out the death signal. The results show DSP can reduce apoptosis by interfering with Fas/FasL expression, protecting the cells from damage by hypoxia and deoxygenation/re-oxygenation.

4. Effects on Lipidemia and Atherosclerosis in Rabbits

The testing showed that DSP can lower TC, TG, LDL-C, VLDL-C concentration, and TC/HDL-C ratio in the blood serum in rabbits. DSP also reduced the thickness of the aortic spot plate and the area of the aortic spot plates. DSP could adjust lipoprotein level and prevent atherosclerosis to a certain extent.

5. Anti-oxidation and Removal of Free Radicals

By comparing the effect of Diltiazem and the effects of DSP on M-IR and its correlated biochemical markers, MDA and SOD can be observed. The SOD activity of the DSP group increased. There was an obvious difference when compared with the control group (P□0.01). DSP provides protection from injuries caused by reperfusion of the ischemic area and increases the activity of SOD. MDA is the main catabolic product of the oxidation of fats. It can damage the structure of the cell membrane so seriously that heart and liver tissue are damaged. SOD has an effective action of clearance on superoxide anions. It can regulate the oxidation reaction controlled by free radicals. DSP can increase SOD activity, decrease MDA content, lower the oxidation standard, and reduce the level of damage to the organs.

6. Effects on Cardiac Arrhythmia Caused by Exogenous Free Radicals

Langendorff perfusion device was used to pour ferrous sulfate (0.25 mmol/L)/citrate (1.0 mmol/L) into the Wistar rat's artificial heart. The model of free radicals causing heart rhythm irregularity was replicated to observe the effects of DSP. Exogenous free radicals can increase cardiac arrhythmia up to 100% and atrial cellular lysis up to 43%. 1 mg/L verapamil and 50 mg/L DSP can lower the irregularity percentage to 71.4% and 87.5%. It shows that DSP can prevent cardiac arrhythmia caused by free radicals.

7. Clinical Applications for Acute Pancreatitis in Rats

This experiment uses the acute pancreatitis model with multi-organ malfunction in rats to show the change in the blood plasma endothelins and the clinical applications of DSP. The experiment shows that blood plasma ET content increases significantly in acute pancreatitis with malfunction of multiple organs. Blood plasma ET content decreases significantly after DSP treatment, and treatment can greatly improve liver, kidney and pancreas function.

8. Prevention of Platelet Aggregation and Thrombosis

The increasing of cAMP inhibits the activity of phosphoesterase and epoxidase, and reduces the production of prostaglandin peroxide. It can also activate protease to phosphoesterize the membrane protein, alter the effects of membrane protein composition on platelet aggregation, and control platelet aggregation to prevent thrombosis. DSP can increase blood platelet concentration and plasma camp content in order to prevent thrombosis.

9. Effects of DSP on Blood Vessels and Nerve Lesion in Diabetic Rats

DSP cannot thoroughly protect blood vessels and nerves or prevent the occurrence of blood vessel and nerve lesion in diabetic rats, but it can relieve or reduce its occurrence in the 6 month-diabetic rat, especially in terms of protein in the urine and lesion of blood capillaries of the kidneys and retina. This may be related to the function of DSP, which can increase thrombolysis.

Clinical Research on Dan Shen Pill

1. Treatment of Coronary Heart Disease with DSP

(1) Ordinary Treatment of Coronary Heart Disease with DSP

After DSP became available in the market in China, a large-scale clinical research project was conducted in China. Although different prescriptions were used in different research projects, all clinical and experimental markers were standardized. The effects of DSP on the treatment of coronary heart disease are much better than that of Dan Shen tablet statistically. The treatment is basically similar to that of Isordil and there is no significant difference between them statistically. DSP works efficiently in small dosages. It is convenient, safe, easily absorbed, and has no side effects.

(2) Pain-killing Effects of DSP on Coronary Heart Disease Compared with Glyceryl Trinitrate

The above experiment shows that the effects of DSP treatment on coronary heart disease are similar to that of glyceryl trinitrate. The results of both ECGs are similar 30 mins after treatment, and the Chinese classification of coronary heart disease does not affect the efficacy of DSP.

(3) Effects of DSP on the Onset of Coronary Heart Disease, Heart Pain Frequency and Volume of Glyceryl Trinitrate Used

The results show that DSP can reduce onset frequency and volume of glyceryl trinitrate used. The level and duration of pain improved after a certain period of treatment, and the onset frequency also decreased. This explains why DSP can improve blood flow to the heart in addition to relieving pain.

(4) Improvement of Blood Pressure and Cardiac Function in Patients with Coronary Heart Disease

The results prove that DSP can improve cardiac function in patients with coronary heart disease and provide improvements in blood flow.

(5) Effects of DSP on ECGs and Blood Flow in Patients with Coronary Heart Disease

No significant differences appeared on ECGs and average exercise testing standards to show improvement from DSP and Isordil (P□0.05), but the average exercise testing standards in the DSP group were much better before and after treatment (P□0.01). This test proves that the treatment effects of DSP on coronary heart disease are the same as that of Isordil with no side effects and increase in tolerance. Also, DSP controls irregular blood flow, lowers blood viscosity, reduces the occurrence of atherosclerosis, and prevents thrombosis much better than Isordil and can be the first choice for the treatment of coronary heart disease.

(6) Effects of Long-term DSP Treatment on Coronary Heart Disease

Long-term DSP results are stable, and there is no antibiotic resistance. Isordil can efficiently lower blood pressure, leading to the activation of endogenous nerve and body fluid system and an increase in blood volume. In addition, Isordil works on sulfur radicals inside the capillary wall, but it would consume sulfur radicals in the long term and reduce treatment effects. DSP is a multi-level, multi-subjected and multi-method medicine which improves cardiac muscle; increases blood volume by blocking the chronic calcium route; stabilizes the myocardial membrane; removes free radials; regulates myocardial cells metabolism; improves blood platelets aggregation; and lowers cholesterol and blood viscosity. Therefore, long-term DSP treatment gives significant treatment effects.

(7) Clinical Research on the Effects of DSP on Unstable-type Angina.

The experiment shows that DSP can reduce oxygen consumption by cardiac muscles, improve blood flow in coronary arteries, and rebalance the oxygen demand-to-oxygen supply ratio in cardiac muscles.

(8) The Effects of DSP on the Treatment of Exertion-type Angina

DSP can efficiently relieve pain and increase blood flow to the cardiac muscle. DSP can also reduce oxygen consumption, improve blood flow to the coronary artery, rebalance oxygen demand and oxygen supply, and prevent atherosclerosis. It is the ideal medicine for the prevention or treatment of coronary heart disease, angina and atherosclerosis.

(9) Research on Senior Group Angina

Both DSP and Nifedipine can treat angina caused by coronary heart disease, but the latter has side effects which are not suitable for long-term use. In order to choose suitable drugs for patients with a need for long-term treatment of coronary heart disease, a comparative analysis of DSP and Nifedipine in the treatment of angina caused by coronary heart disease was carried out. DSP is made for angina. It activates blood circulation and relieves pain efficiently. Its effects are long lasting, require only a small dosage and have no side effects. Nifedipine is a short-term-effective calcium antagonist with a short half-life and functional time, so angina may occur during medication. It also has many side effects. Many reports state that long-term treatment with Nifedipine is harmful to coronary arteries. DSP can prevent decreased blood flow to the cardiac muscles and the development of atherosclerosis.

2. Effects on Cardiac Arrhythmia

The treatment effects of DSP on cardiac arrhythmia caused by coronary heart disease are significant. It is also helpful to those patients without heart disease. Its functions are: a) calcification. DSP can reduce intracellular calcium concentration and prevent calcium overloading better than verapamil. b) Stabilizing the cell membrane. DSP can protect cardiac muscle and regulate heart rhythm. c) Removal of free radicals. d) Speeding up energy production and utilization. There is no relationship between chronic irregularity of heart rhythm and the addition of resistance and lack of energy supply.

DSP and Di'ao Xinxuekang can both improve cardiac arrhythmia caused by myocarditis and heart malfunction, but DSP does a better job than Di'ao Xinxuekang. DSP can improve blood flow to the cardiac muscles, section ST and T wave in ECGs. In addition, DSP can also reduce platelet aggregation, and platelet viscosity. The results show that patients who take DSP in the long term enjoy relief from symptoms and low reoccurrence of myocarditis.

3. Reverse Function of DSP on Left Ventricular Hypertrophy (LVH)

The above experiment shows that DSP prevents damage caused by free radicals, prevents atherosclerosis, improves blood circulation, decreases blood viscosity and exterior blood vessel resistance, and regulates compliance of cardiac muscles to reverse LVH.

4. DSP Treatment for High Blood Pressure

The experiment shows that DSP can stop and improve LVH and dilate the left ventricle, which can then lower blood pressure and combat angina.

Besides controlling blood pressure efficiently, other important steps for treating high blood pressure include: increasing the reactivity of insulin, lowering insulin level, and improving ET function in blood vessels. DSP is helpful because it also lowers blood pressure.

5. Treatment of Hyperlipidaemia

This research shows that DSP can significantly lower blood lipoprotein level and improve blood flow, especially by the thinning of IMT after treatment. It explains how this drug can prevent atherosclerosis besides providing the above functions. DSP is safe and effective for older patients with coronary heart disease, angina and high blood viscosity.

6. Treatment for Hyperviscosity Syndrome (HS)

Hyperviscosity Syndrome (HS) is a pathobiological concept, a syndrome caused by one or more blood viscosity factor(s). It can lead to lack of blood supply, hypoxia, blocking, etc. in the heart, brain and kidneys. DSP offers the best results in HS treatment. After the normal 28 days of medication, HS symptoms such as nausea, lack of energy, breath holding, anxiety, etc. related to coronary heart disease, cerebral infraction, and kidney disease disappeared gradually. Blood pressure was lowered, and blood circulation improved. TC, TG, Apo-B dropped, and HDLC and Apo-A1 rose. All levels of hemorheology markers dropped. Renal Blood flow increased, and renal function improved. Urine protein decreased, and cardiac function improved.

7. Treatment for Acute Myocardial Infarction (AMI)

DSP can improve blood circulation by dilating coronary arteries, saving cardiac muscle, minimizing the infarction area, and protecting myocardial cells. Therefore, DSP can protect cardiac muscles in the early stages of AMI. It is a convenient medication with no side effects, which is recommended in the clinical field.

8. Effects on Treatment of Cerebral Infarction

The use of DSP to treat low blood supply to the brain, cerebral infarction and internal bleeding is very efficient.

9. Effects on Blood Micro-circulation

The experimental results show that DSP can make an improvement in bulbar conjunctiva microcirculation and thrombo-elasticity in patients with coronary heart disease and angina.

10. Effects on Immunity of Red Blood Cells

This experiment uses the blood coagulation method of yeasts sensitized by complement, C_(3b)-causing yeast aggregation testing and Enzyme-linked Immunosorbent Assay (ELISA), to test the effects of DSP on the immunosorbent ability of red blood cells, CIC, and SIL-2R in patients with coronary heart disease. The experiment shows that DSP can lower SIL-2R level, strengthen the immune system and the immunosorbent ability of red blood cells.

11. Adjustment of Vegetative Nerve

This test uses “Wenger-Chongzhongchongxion” vegetative nerve balance factor analysis to test the heart rate variation (HRV), that is, the fluctuation in the average heartbeat over a certain period of time or over a long time period in the R-R period. Data, including effects on the sympathetic and para-sympathetic nerves can be calculated, to reflect the regulatory function of the vegetative nervous system. After DSP treatment, the percentage of y>+0.56 dropped significantly (P□0.05), but the drop in the Isordil group before and after treatment was not significant, y>+0.56 (P□0.05). After DSP treatment, SDNN in R-R increased significantly (P<0.01), and there was no significant difference in the Isordil group before and after treatment (P□0.05). A decrease in HRV means the sympathetic nerve is excited. It is directly proportional to the symptoms in coronary heart disease and the possibility of sudden death and irregularity of heartbeat. DSP can control over-excitement of the para-sympathetic nerve and regulate the balance in the vegetative nerve.

12. DSP Treatment for Liver Disease

There is significant improvement in the treatment of hepatocirrhosis at the stage of losing compensation when DPS is added as a medication. DSP does not have side effects and is helpful in treating hepatocirrhosis.

13. The Effectiveness of DSP Therapy in Diabetes and Related Complications

Trial results reveal that after 3 months of taking DSP, the 40 patients' nail wall microcirculation test indexes had varying degrees of improvement. Their collective cumulative values decreased. Among the patients, those originally with serious abnormalities now had medium abnormality; those originally with medium abnormality had slight abnormalities. The differences before and after treatment were obvious. DSP has positive healing effects on diabetic end-brush neuritis.

14. The Effectiveness of DSP Therapy on Optical Fundus Vascular Diseases

The cause of retinal vein occlusion is still not very clear. Hypertension, hyperlipidemia, and arteriosclerosis are usually considered as likely causes of retinal vein occlusion. Doctors of traditional Chinese medicine believe that it is caused by stagnant blood flow. DSP can activate blood circulation and relieve congestion, improve microcirculation, relieve hydropsy, and encourage blood absorption. In so doing, it can improve eyesight. DSP can also be used to heal different kinds of optical fundus vascular diseases that are generally termed as Xueyuzheng, such as central retinal artery occlusion, hypertensive retinal arteriosclerosis, diabetic retinal lesion, central plasm optic neuropathy, central permeation optic neuropathy, ischemic optic neuropathy, optic neuritis, atrophy of the optic nerve, etc.

15. DSP's Effect on Hemorheology

In the Observation group, besides fibrinogen, whole blood viscosity, whole blood reduction viscosity, plasma viscosity, hematocrit and Aggregation Index of RBC all decreased. The differences before and after treatment were obvious (P<0.05 or P<0.01). Compared with the Control group, whole blood viscosity, whole blood reduction viscosity, plasma viscosity, and Aggregation Index of RBC had obvious decreases (P<0.05 or P<0.01). After treatment, the Control group shared an obvious change only in the hemagglutilation index (P<0.05 or P<0.01).

16. DSP's Healing Effect on Chronic Pulmonary Heart Disease

The total efficacy rate of treatment group is 95% and that of the control group 76%, the difference of which is statistically significant (P□0.05). The result revealed that the efficacy of DSP is superior to persantin and that hemorheology in the DSP group has more improvement than that in the persantin group. There was a significant difference in the efficacy of the two groups (X²=4.46 and 4.95, P□0.05). Treatment group results were better than that of the Control group. There were obvious changes in blood flow in the Treatment group before and after treatment compared with that of the Control group (P□0.05). The blood viscosity of the control group decreased after treatment, but there was no statistical deviation.

17. Treatment of Adrenal Syndrome

The results show that the complete reversal percentage and total efficacy in the treatment group were 55% and 90%, respectively, which was significantly higher than those in the control group: 27.5% and 65% (P□0.05). DSP, combined with other medications, can improve treatment results and reduce the percentage of reoccurrence.

18. Treatment of Other Diseases

(1) Treatment of bronchitis in children. DSP combined with antibiotics can improve treatment results in infections. The DSP treatment ended fever and rales better than that of the control group. DSP raised the recovery percentage for pneumonia in children and shortened the duration of treatment without significant side effects.

(2) Effects on hemicrania. 58 patients with hemicrania were selected from clinics. The result shows that the efficacy in the treatment group is higher than that of the control group (P□0.05). DSP can efficiently cure and prevent hemicrania.

(3) Treatment of chronic gastritis. DSP can regulate the function of blood vessels, restrain platelet aggregation, control thrombosis, clear out stagnant blood in the gastric mucosa and cure stomachache caused by chronic gastritis. It can efficiently eliminate the dead parts of the erosive gastric mucinitis, activate megakaryocytes, and stimulate production of new cells to improve the recovery from inflammation.

(4) Treatment of dizziness. The total efficacy in the Treatment group and the Control group were 86% and 87.5%, respectively. No significant abnormality was found. These two groups of drugs can treat fainting efficiently. Therefore, DSP can be a convenient and efficient drug to treat fainting caused by insufficient blood supply to the brain.

(5) Treatment of damaged lateral malleolus joint. DSP can eliminate swelling and stagnant blood, and can kill pain. One active ingredient, borneol, can increase DSP's absorption through the skin and maintain concentrations of the drug at the application site, so it can efficiently and quickly treat damage of the lateral malleolus joint. It is helpful in treating broken bones, bone death and proliferation of bone.

(6) Prevention and treatment of plateau hypoxia. Plateau hypoxia can lead to capillary circulation disorder, causing blood-perfusing insufficiency. Plateau hypoxia also leads to high blood viscosity, increased red blood cell quantity—and red blood cell aggregation, enhanced red blood cell rigidity, increased platelet aggregation, and change in pH value. All the above factors affect blood viscosity and the radius of capillaries. Platelet aggregation can increase resistance in capillaries, leading to blockage. When blood viscosity increases, the radius of capillaries also increases and leads to increased resistance and congestion. There are common properties in the blood flow of people with plateau hypoxia: “concentration” (increased red blood cell pressure), “viscosity” (increased whole blood viscosity), and “aggregation” (increased aggregation of red blood cells). All the above are different at different sea levels and durations. Forementioned pharmaphysiologic and clinical research show that DSP can lower hematocrit, blood sedimentation and blood viscosity, so it is helpful in preventing and treating plateau hypoxia.

(7) Prevention and treatment of Senile dementia. Senile dementia can be classified as Alzheimer's Disease (AD), vascular dementia and combined dementia. After DSP treatment, there is statistically significant improvement in AD and vascular dementia by measurement analysis and Chinese medicine clinical observation (p<0.05 or p<0.01). DSP is helpful for treating sluggishness, reticence, forgetfulness, fatigue, and ecchymosis at a total efficacy of 40%, and sadness, anger, rashness, and irritation at a total efficacy of 85.7%.

This invention will be better understood from the examples which follow. However, one skilled in the art will readily appreciate that the specific methods and results discussed are merely illustrative of the invention as described more fully in the claims which follow thereafter.

EXAMPLE 1

41.06 g of Radix Salviae Miltiorrhizae, 8.03 g of Radix Notoginseng were respectively weighed and ground and then sequentially introduced into an extractor. 5 parts water were added. The mixture was decocted for 2 hours, filtered, and the first filtrate was removed. The residue was added to 4 parts water, decocted for 1 hour, filtered, and then this second filtrate was mixed with the first filtrate. The mixed filtrate was concentrated under decompressed conditions until the solution volume (L) to raw materials weight (Kg) ratio was about 0.9-1.1. 95% ethanol was gradually poured in until the concentration of ethanol was 69-71%. This was settled for 12 hours and filtered. The filtrate, in which ethanol is evaporated, is concentrated to extract of the relative of 1.32-1.40.

The above extract was mixed with 0.46 g of borneol and 18 g of polyethylene glycol 6000. The mixture was heated to 85° C., melted for 30 minutes, and then transferred to a dropping machine at 80° C. The melted mixture was dropped into the liquid paraffin, at a temperature of 7° C. The dropping pills were taken out, and the oil was removed.

The dropping pill is a reddish brown-brownish black sphere with an even size, smooth color, scent, and bitter taste. The weight per pill is 25 mg±15%, and the diameter per pill is 3.34±15% mm.

The above dropping pill contains the following active ingredients: Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

EXAMPLE 2

31.12 g of Radix Salviae Miltiorrhizae, 9.21 g of Radix Notoginseng, 0.50 g of borneol and 20 g of polyethylene glycol 6000 were processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 64° C., and the temperature of the liquid paraffin was 0° C.

The dropping pill is a reddish brown-brownish black sphere with an even size, smooth color, distinct scent, and bitter taste. The weight per pill is 25 mg±15%, and the diameter per pill is 3.34±15% mm.

The above dropping pill contains the following 5 active ingredients: Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

EXAMPLE 3

59.36 g of Radix Salviae Miltiorrhizae, 6.38 g of Radix Notoginseng, 0.34 g of borneol and 21 of polyethylene glycol 6000 were taken and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 69° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

The dropping pill is a reddish brown-brownish black sphere with an even size, smooth color, distinct scent, and bitter taste. The weight per pill is 25 mg±15%, and the diameter per pill is 3.86±15% mm.

The above dropping pill contains the following active ingredients: Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

EXAMPLE 4

59.36 g of Radix Salviae Miltiorrhizae, 6.38 g of Radix Notoginseng, 0.34 g of borneol, 40 g of xylitol and 8 g of starch were processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of dropping machine was at 69° C., the temperature of polymethyl siloxane as condensation liquid was at 4° C.

The dropping pill is a reddish brown-brownish black sphere with an even size, smooth color, distinct scent, and bitter taste. The weight per pill is 35 mg±15%, and the diameter per pill is 3.86±15% mm.

The above dropping pill contains following active ingredients: Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

EXAMPLE 5

Extraction of water-soluble saponins of Panax Notoginseng Radix Notoginseng were weighed and ground, and then introduced into an extractor. 6 parts water was added and decocted for 2 hours with the air pressure between 0.04-0.06 mPa, filtered with 100-mesh net, and the first filtrate was removed. The residue was repeated under the same conditions for 1.5 hours and the second filtrate was removed. Two filtrates were mixed and the filtrate was refined using macroporous adsorption resin eluting with ethanol. The eluate is concentrated under decompressed conditions with the air input to 0.04-0.06 mPa and the vacuum to −0.076˜−0.088 mPa until the density was 1.33-1.35, thereby extracting water-soluble saponins of Panax Notoginseng.

EXAMPLE 6

Extraction of Water-soluble Phenolic Acids of Radix Salviae Miltorrhizae

Radix Salviae Miltorrhizae were weighed and ground, and then introduced into an extractor. 6 parts water was added decocted for 2 hours with the air pressure between 0.04-0.06 mPa, filtered with 100-mesh net, and the first filtrate is got. The residue is repeated under the same condition for 1.5 hours and the second filtrate is got. Two filtrates are mixed and concentrated under decompressed conditions with the vacuum pressure −0.076˜-0.088 mPa until one Kg initial herb becomes one liter. The concentrated solution is precipitated with ethanol and filtered with 100-mesh net. The filtrate is concentrated under decompressed conditions with input air pressure 0.04-0.06 mPa and the vacuum pressure 0.076˜−0.088 mPa, and refined by polyamide chromatography eluting with ethanol. The eluate is concentrated under decompressed condition with the air input to 0.04-0.06 mPa and the vacuum to −0.076˜−0.088 mPa until the density is 1.33-1.35, thereby extract of of water-soluble phenolic acids of Radix Salviae Miltorrhizae is got.

EXAMPLE 7

4.0 g of the extract of water-soluable saponins of Panax Notoginseng from Example 5, 20.6 g of the extract of water-soluble phenolic acids of Radix Salviae Miltorrhizae from Example and 6, 1.9 g of borneol and 79.5 g of polyethylene glycol 6000 are mixed. The mixture is heated to 89° C., melted for 25 mins, and then transferred to a dropping machine at 80° C. The melted mixture is dropped into the liquid paraffin, at a temperature of 8° C. The dropping pills are taken out and, the oil is removed.

The above dropping pill contains the following ingredients: Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1 and Borneol, etc.

EXAMPLE 8

5.8 g of the extract of water-soluble saponins of Panax Notoginseng from Example 5, 50.2 g of the extract of water-soluble phenolic acids of Radix Salviae Miltorrhizae from Example 6, 0.8 g of borneol, and 82.4 g of polyethylene glycol 6000 are mixed, and processed according to Example 7.

It has been shown in tests that the above dropping pill contains the following active ingredients: Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.

EXAMPLE 9

50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁, 15 mg of d-Borneol and 265 mg of polyethylene glycol 6000 were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 64° C., and the temperature of the liquid paraffin was 4° C.

EXAMPLE 10

80 mg of Magnesium Salvianolate B, 10 mg of Ginsenoside Rb₁, 10 mg of d-Borneol and 245 mg of polyethylene glycol 6000 were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of dropping machine was 69° C., and the temperature of the liquid paraffin was 5° C.

EXAMPLE 11

60 mg of Magnesium Salvianolate B, 25 mg of Ginsenoside Rb₁, 8 mg of d-Borneol, 200 g of xylitol and 48 g of starch were mixed, and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 12

30 mg of sodium 3′4-dihydroxyphenyllactate, 40 mg of Ginsenoside Rb₁, 15 mg of d-Borneol, 180 g of lactobacillus and 58 g of starch were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of liquid paraffin was 4° C.

EXAMPLE 13

50 mg of sodium 3′4-dihydroxyphenyllactate, 30 mg of Ginsenoside Rb₁, 10 mg of d-Borneol and 250 g of polyethylene glycol 6000 were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of the liquid paraffin was 4° C.

EXAMPLE 14

40 mg of sodium 3′4-dihydroxyphenyllactate, 25 mg of Ginsenoside Rb₁, 8 mg of d-Borneol, 200 g of lactobacilius and 35 g of starch were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 15

25 mg of sodium 3′4-dihydroxyphenyllactate, 45 mg of Ginsenoside Rb₁, 12 mg of d-Borneol, 185 g of xylitol and 30 g of starch were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 16

20 mg of methyl tanshinonate, 15 mg of ginsenoside Rd, 35 mg of ginsenoside Re, 15 mg of d-Borneol, 245 mg of polyethylene glycol 6000 were mixed and processed according to the extraction and preparation method of Example 1, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 17

10 mg of rosmarinic acid, 15 mg of methyl rosmarinate, 20 mg of tanshinone IIA, 25 mg of ginsenoside Rg2, 15 mg of d-Borneol, 215 g of lactobacillus and 30 g of starch were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 82° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 18

12 mg of Salvianolic acid C, 15 mg of Salvianolic acid E, 20 mg of ginsenoside Rh1, 15 mg of ginsenoside Rh2, 15 mg of d-Borneol, 210 g of lactobacillus and 30 g of starch were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 19

8 mg of Salvianolic acid D, 10 mg of Salvianolic acid G, 15 mg of Salvianolic acid I, 30 mg of ginsenoside Rg3, 15 mg of d-Borneol, 245 mg of polyethylene glycol 6000 were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 79° C., and the temperature of the liquid paraffin as condensation liquid was 4° C.

EXAMPLE 20

8 mg of tanshinone IIB, 15 mg of tanshinone I, 8 mg of dimethyl lithospermate, 15 mg of protocatechualdehyde, 15 mg of notoginsenoside R2, 10 mg of notoginsenoside-R3, 15 mg of d-Borneol, 210 g of lactobacillus and 30 g of starch were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 85° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 21

8 mg of tanshinone V, 12 mg of isotanshinone, 8 mg of monomethyl lithospermate, 10 mg of notoginsenoside R4, 25 mg of ginsenoside Rg1, 15 mg of l-Borneol, 210 g of xylitol and 30 g of starch were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 22

8 mg of tanshinone VI, 5 mg of 1-dehydrotanshinone, 5 mg of neocryptotanshinone, 15 mg of ethyl lithospermate, 10 mg of notoginsenoside R6, 15 mg of Salvianolic acid A, 15 mg of d-Borneol, 245 mg of polyethylene glycol 6000 were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of the liquid paraffin as condensation liquid was 4° C.

EXAMPLE 23

25 mg of lithospermic acid B, 15 mg of dihydrotanshinone, 40 mg of ginsenoside Rb1, 10 mg of notoginsenoside R7, 15 mg of d-Borneol, 215 g of xylitol and 30 g of starch were mixed and processed according to the extraction and preparation method of Example 7, except for the difference in parameters as follows: the temperature of the dropping machine was 80° C., and the temperature of polymethyl siloxane as condensation liquid was 4° C.

EXAMPLE 24

Magnesium Salvianolate B was extracted by steps of:

-   -   (1) Pulverizing Salvia miltiorrhiza Beg. into a fine powder and         decocting twice with hot water;     -   (2) Combining the decoctions and concentrating in vacuum under         50° C.;     -   (3) Loading the solution from the step (2) into macroporous         adsorption resin and, after washing with water, eluting column         with 40% ethanol;     -   (4) After recovering the ethanol from solution obtained in the         step (3), refining it by Sephadex LH-20 or other gel columns         with similar characteristics, eluting with ethanol and         collecting eluant containing Magnesium Salvianolate B.     -   (5) Repeating the process of step (4) until the concentration of         Magnesium Salvianolate B reaches more than 90%.

EXAMPLE 25

Ginsenoside Rb₁ was extracted by steps of:

-   -   (1) Pulverizing Panax notoginseng or Ginseng into a fine powder,         and decocting with water; or refluxing with 70% ethanol; or         percolating with 70% ethanol;     -   (2) Recovering solvent from the solution at reduced pressure;     -   (3) Loading the solution from step (2) into macroporous         adsorption resin and, after washing with water, eluting column         with 40% ethanol;     -   (4) After recovering the ethanol from the solution obtained in         step (3), refining it by silica gel column;     -   (5) Eluting the column with chloroform, methanol and water in         the ratio of 6:3:1, respectively, and collecting the eluant;     -   (6) Using TLC for examination of Ginsenoside Rb₁ and recovering         the solvent, thereby obtaining Ginsenoside Rb₁.

EXAMPLE 26

6 mg of tanshinoneII A, 10 mg of Salvianolic acid A, 8 mg of lithospermic acid B, 25 mg of ginsenoside-Rg1, 12 mg of d-Borneol, 40 g of microcrystalline cellulose, 0.5 g of tale powder and appropriate amount of 3% polyvidone in ethanol solution were taken and made into tablets according to standard procedures.

EXAMPLE 27

10 mg of rosmarinic acid, 30 mg of sodium 3′4-dihydroxyphenyllactate, 10 mg of ginsenoside-Rg3, 20 mg of notoginsenoside-R1, 8 mg of d-Borneol, 50 g of gelatin and 10 g of glycerin were taken and made into capsules according common practices.

EXAMPLE 28

Salvianolic acid A, ethyl lithospermate, ginsenoside-Re, notoginsenoside-R3, 10 mg of d-Borneol, 30 g of magnesium stearate, 15 g of starch and an appropriate amount of 3% polyvidone in ethanol solution were taken and made into granules according to routine procedures.

EXAMPLE 29

10 mg of lithospermic acid, 20 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of ginsenoside-Rg3, 8 mg of d-Borneol, 35 g of microcrystalline cellulose, 10 g of starch and an appropriate amount of 3% polyvidone in ethanol solution were taken and made into pills according to routine procedures.

EXAMPLE 30

60 mg of Salvianolic acid B, 10 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of Ginsenoside Rb₁, 10 mg of d-Borneol, 30 mg of mannitol and 5 mg of antallin and an appropriate amount of water were taken and made into a sterile powder for treating infection according to routine procedures. 

1. A composition for treatment of heart disease comprising the extract of raw herbs of Radix Salviae Miltorrhizae, Panax Notoginseng and Borneol.
 2. A composition of claim 1 comprising herb extracts from raw herbs of 80.0-97.0% Radix Salviae Miltorrhizae, 1.0-19.0% Panax Notoginseng and 0.1-1.0% Borneol.
 3. The composition of claim 1 comprising extracts from raw herbs of 90.0-97.0% Radix Salviae Miltorrhizae, 2.5-9.6% Panax Notoginseng and 0.2-0.5% Borneol.
 4. The composition according to claim 1 comprising extracts from raw herbs of 89.8% Radix Salviae Miltorrhizae, 9.6% Panax Notoginseng and 0.5% Borneol.
 5. The composition according to claim 1, 2, 3, or 4, produced by the steps of: a. obtaining an appropriate amount of smashed Radix Salviae Miltorrhizae and Panax Notoginseng; b. Extracting the obtained Radix Salviae Miltorrhizae, and Panax Notoginseng in hot aqueous reflux at about 60-100° C.; c. Filtering and combining the extracts to form a combined extract; d. Concentrating the combined extract from step (c) into an appropriate ratio of the volume of the concentrated extract to the weight of the inputted herbal materials to form a concentrated extract; e. Putting ethanol into the concentrated extract from step (d) to about 50-85% final concentration of ethanol, performing ethanol precipitation and forming a precipitated resolution; f. Concentrating the supernatant liquid of the precipitated resulting from step (e) to form a plaster of about 1.15-1.45 in relative density; and g. Mixing the plaster from step (f) with an appropriate amount of Borneol, thereby producing the composition of herb extract of Radix Salviae Miltorrhizae, Panax Notoginseng and Borneol.
 6. The composition according to claim 1, 2, 3, or 4, comprising Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, and Borneol.
 7. A composition for treatment of chronic stable angina pectoris, comprising 5-40% water-soluble phenolic acid of Radix Salviae Miltorrhizae, 1-10% water-soluble saponin of Panax Notoginseng and 1-5% of Borneol.
 8. The composition according to claim 7, comprising 10-30% water-soluble phenolic acid of Radix Salviae Miltorrhizae, 2-6% water-soluble saponin of Panax Notoginseng and 1-3% of Borneol.
 9. A composition capable of treating chronic stable angina pectoris comprising about 0.14 to about 0.18 mg Danshensu per pill, at least 12.12 μg Sanchinoside R1 per pill and at least 56.26 μg Ginsenoside Rg1 per pill.
 10. The composition according to claim 7, 8, or 9, produced by steps of: a. Extracting Radix Salviae Miltorrhizae, Panax Notoginseng separately in hot aqueous reflux and filtering separately; b. Concentrating filtrates separately; c. Refining the concentrates separately using resin columns and concentrating, and getting refined water-soluble extract of Radix Salviae Miltorrhizae and refined water-soluble extract of Panax Notoginseng; and d. Mixing the refined water-soluble extracts from step (c) with an appropriate amount of borneol, thereby producing a composition capable of treating chronic stable angina pectoris.
 11. The composition according to claim 10, produced by steps of: (1) Extraction of water-soluble components of Panax Notoginseng a. Diluting herbs with 5-7 parts of water; b. Extracting water-soluble components of Panax Notoginseng by boiling in a tank with the air pressure between 0.04-0.06 mPa for 2 hours; c. Repeating extraction under the same conditions for 1.5 hours; d. Filtering of the extraction with 100-mesh net; e. Refining the filtrate using macroporous adsorption resin eluting with ethanol; and f. Concentrating the eluted extracts under decompressed conditions with the air input to 0.04-0.06 mPa and the vacuum to −0.076˜−0.088 mPa until the density is 1.33-1.35; (2) Extraction of water-soluble components of Radix Salviae Miltorrhizae a. Diluting herbs with 5-7 parts of water; b. Extracting water-soluble components of Radix Salviae Miltorrhizae by boiling in a tank with the air pressure between 0.04-0.06 mPa for 2 hours; c. Repeating extraction under the same conditions for 1.5 hours; d. Filtering the extraction with 100-mesh net; e. Concentrating the filtrates under decompressed conditions with the vacuum pressure −0.076˜−0.088 mPa until one Kg initial herb becomes one liter; f. Precipitating the concentrates with ethanol; g. Filtering the ethanol precipitates solution through 100-mesh net; h. Concentrating the filtrates under decompressed conditions with input air pressure 0.04-0.06 mPa and the vacuum pressure 0.076˜31 0.088 mPa; i. Refining the concentrates by polyamide chromatography, eluting with ethanol; and j. Concentrating the refined extracts to the density of 1.33-1.35; (3) Producing the pill a. Mixing the extracts of Panax Notoginseng, the extracts of Radix Salviae Miltorrhizae, synthetic borneol and polyethylene glycol 6000 at the ratio of 4.0:20.6:1.9:79.5; b. Melting the mixture; c. Manufacturing the melted mixture to pills using the dropping machine with the following characteristics: the temperature of dropping pot is constantly 89-93° C., the cooling solution is liquid paraffin with a temperature lower than 8° C., the inner diameter of the dropping head is 1.8 mm, the outer diameter of the dropping head is 2.4 mm, the distance between the dropping head and the surface of cooling solution is 15 cm; and d. Centrifugation of the pills at 800-1100 rpm for 15 minutes to remove oils.
 12. The composition for the treatment of chronic stable angina pectoris comprising Sodium 3′4-dihydroxyphenyllactate, Protocatechuic Aldehyde, Salvianolic acid A, B, C, D, E, F, Rosemarinic acid, Ginsenoside Rg1, Ginsenoside Rb1, Ginsenoside Re, Notoginsenoside R1, Borneol, etc.
 13. A composition for the treatment of heart disease comprising active ingredients extracted from Salvia miltiorrhiza Beg., Panax notoginseng or Ginseng, and Dryobalanops aromatica Geartu.F. or Cinnammon camphor., wherein the active ingredient extracted from Salvia miltiorrhiza Beg. consists of one or more ingredients selected from the group as follows: tanshinone, salvianolic acid, methyl tanshinonate, rosmarinic acid, methyl rosmarinate, danshexinkum, protocatechualdehyde, Sodium 3′4-dihydroxyphenyllactate, lithospermic acid; the active ingredient extracted from Panax notoginseng or Ginseng consisting of one or more ingredients selected from notoginsenoside and ginsenoside; the active ingredient extracted from Dryobalanops aromatica Geartu.F. or Cinnammon camphor selected from d-borneol or l-borneol or both of them.
 14. The composition according to claim 13, wherein the said tanshinone is one or more ingredients selected from the group as follows: tanshinone I, tanshinone IIA, tanshinone IIB, tanshinone V, tanshinone VI, isotanshinone, miltirone, dihydrotanshinone, 1-dehydrotanshinone, and neocryptotanshinone.
 15. The composition according to claim 13, wherein the said salvianolic acid is one or more ingredients selected from the group as follows: Salvianolic acid A, Salvianolic acid B, Salvianolic acid C, Salvianolic acid D, Salvianolic acid E, Salvianolic acid G, and Salvianolic acid I.
 16. The composition according to claim 13, wherein the said lithospermic acid is one or more ingredients selected from the group as follows: lithospermic acid B, ethyl lithospermate, dimethyl lithospermate, and monomethyl lithospermate.
 17. The composition according to claim 13, wherein the ginsenoside is one or more ingredients selected from the group as follows: ginsenoside Rb1, ginsenoside Rd, ginsenoside Re, ginsenoside Rg1, ginsenoside Rg2, ginsenoside Rg3, ginsenoside Rh1, and ginsenoside Rh2.
 18. The composition according to claim 13, wherein the said notoginsenoside is one or more ingredients selected from the group as follows: notoginsenoside R1, notoginsenoside R2, notoginsenoside-R3, notoginsenoside R4, notoginsenoside R6, and notoginsenoside R7.
 19. The composition according to claim 13, characterized by comprising Magnesium Salvianolate B or 3′4-dihydroxyphenyllactate extracted from the Salvia miltiorrhiza Beg., Ginsenoside Rb₁ extracted from the Panax notoginseng or Ginseng, and d-Borneol extracted from the Dryobalanops aromatica Geartu.F. or Cinnammon camphor.
 20. The composition according to claim 19, characterized by comprising 10-80 mg of Magnesium Salvianolate B, 10-50 mg of Ginsenoside Rb₁ and 5-30 mg of d-Borneol.
 21. The composition according to claim 20, characterized by comprising 50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol.
 22. The composition according to claim 19, characterized by comprising 5-80 mg of sodium 3′4-dihydroxyphenyllactate, 10-50 mg of Ginsenoside Rb₁ and 5-30 mg of d-Borneol.
 23. The composition according to claim 22, characterized by comprising 20 mg of sodium 3′4-dihydroxyphenyllactate, 20 mg of Ginsenoside Rb₁ and 15 mg of d-Borneol.
 24. The composition comprising one or more excipients such as polyethylene glycol, xylitol, lactobacillus, starch for preparation of dripping pills, wherein 50 mg of Magnesium Salvianolate B, 20 mg of Ginsenoside Rb₁, 15 mg of d-Borneol and 265 mg of excipient are contained per ten dripping pill.
 25. The composition according to one of claims 13-24, wherein the Salvianolate B was extracted by steps of: a. Pulverizing Salvia miltiorrhiza Beg. into a fine powder, and decocting twice with hot water; b. Combining the decoctions, and concentrating vacuum conditions under 50° C.; c. Loading the solution from step (b) into macroporous adsorption resin and, after washing with water, eluting column with 40% ethanol; d. After recovering the ethanol from the solution obtained in step (c), refining it by Sephadex LH-20 or other gel columns with similar characteristics, eluting with ethanol and collecting eluant containing Magnesium Salvianolate B; and e. Repeating the process of step (d) until the concentration of Magnesium Salvianolate B reaches more than 90%.
 26. The composition according to one of claim 13-24, wherein the Ginsenoside Rb₁ was extracted by steps of: a. Pulverizing Panax notoginseng or Ginseng into a fine powder, and decocting with water; or refluxing with 70% ethanol; or percolating with 70% ethanol; b. Recovering solvent from the solution at reduced pressure; c. Loading the solution from step (b) into macroporous adsorption resin and, after washing with water, eluting column with 40% ethanol; d. After recovering the ethanol from the solution obtained in step (c), refining it by silica gel column; e. Eluting the column with chloroform, methanol and water in the ratio of 6:3:1, respectively, and collecting eluant; and f. Using TLC for examination of Ginsenoside Rb₁ and recovering the solvent, thereby obtaining Ginsenoside Rb₁.
 27. The composition according to one of claims 13-24, wherein d-Borneol was extracted from trunk of Dryobalanops aromatica Geartu.F. or leaves of Cinnammon camphor. by means of vapor distillation, or supercritical carbon dioxide extraction.
 28. The compositions according to one of claims 1-27, formulated in a dropping pellet, pill, capsule, granule, tablet, suspension, injection, syrup, tincture, powder, tea, topical solution, nebula, suppository microcapsule, or other pharmaceutically acceptable form.
 29. The compositions according to one of claims 1-28, capable of increasing blood volume in coronary artery, relaxing the smooth muscles of blood vessels, improving the peripheral circulation, raising the oxygen content in veins, or significantly improving the acute myocardial ischemia or myocardial infarction, protecting the cells from damage by hypoxia or anoxia, protecting cells suffering from myocardial ischemia, improving micro-circulation, preventing arrhythmia, preventing platelets aggregation, thrombosis and dissolve fibrin, lowering blood viscosity, adjusting the blood cholesterol or preventing atherosclerosis, raising the tolerance to hypoxia or anoxia, preventing the oxidation of lipoprotein or removing the harmful free radicals, lowering plasma ET content, significantly improve the liver, kidneys and pancreas functions, preventing the occurrence or development of blood vessel or nerve diseases, enhancing the immune system, regulating the vascular nervous balance.
 30. The compositions according to one of claims 1-28, capable of preventing and treating cardiovascular and cerebrovascular diseases, kidney disease, liver disease, pneumonia, lung or heart disease, pancreatitis, diabetes, vertebral disease, optic vessels disease, optic nerves disease, eccentric headache, chronic stomachitis, dizziness, bone diseases, altitude diseases, common elderly diseases; treating stable angina pectoris, unstable angina pectoris, aged angina pectoris, non-symptomatic myocardial ischemia, different types of coronary heart diseases or angina pectoris diseases, treating arrhythmia, enlargement of left ventricle, myocarditis, myocardial infarction or cerebral infraction, treating hyperlipidaemia, high blood viscosity syndrome or high blood pressure, treating diseases caused by micro-circulation disorder, treating stroke, cerebral infarction, cerebral bleeding and other cerebral diseases, treating hepatitis B, chronic liver fibrosis, liver fibrosis, active liver cirrosis, liver cirrosis in compensation period and other related diseases, treating kidney syndrome and its conjunctive diseases, treating diabetes or its conjunctive diseases, treating cyanosis-typed optic vessels diseases such as venal blockage in retina, central optic artery blockage in retina, high blood pressure optic atherosclerosis in retina, diabetic retinopathy, cento-neuropathy, cento-osmotic neuropathy, ischemic neuropathy, optic neuritis or optic nervous dystrophy, treating dizziness caused by cerebral-arterial ischemia, Meniere's disease, high blood pressure, coronary heart disease, treating detrimental death of epicondylus medialis, femoral end necrosis, twisted joint, ligament damage, fracture and proliferation of bone cells, treating bronchitis in children, treating hypoxia or anoxia, treating Alzheimer's Disease.
 31. A dropping machine for manufacturing a small-sized medicament comprising any one of compositions of claims 1-28, which can be readily dissolved thus readily delivered to organs, comprising the parts of: a. Dropping pot in which the temperature of liquid is 60-100° C.; b. Apparatus which holds liquid paraffin cooling solution of which temperature is lower than 8° C.; and c. Dropping head with 1.8 mm inner diameter and 2.35 mm outer diameter which distanced from the surface of cooling solution by approximately 15 cm, said dropping head allowing the dropping speed of over 30 pellets per minute.
 32. A method of determining the active fractions of any one of compositions of claims 1-28 which are capable of treating and preventing cardiovascular disease, wherein said method comprising the steps of: a. Fractionating pharmaceutical compositions by high performance liquid chromatography (HPLC); b. Comparing the retention time of the fractions of pharmaceutical compositions with the retention time of saponin R1, saponin Rg1, and saponin Re; and c. Determining if pharmaceutical compositions contain fractions of which retention time is equivalent to the retention time of saponin R1, saponin Rg1, and saponin Re.
 33. A method of determining the active fractions of any one of compositions of claims 1-28 which are capable of treating and preventing cardiovascular disease, wherein said comprising the steps of: a. Fractionating a pharmaceutical composition by thin layer chromatography (TLC); b. Comparing the position and color of the fractions of pharmaceutical compositions with the position and color of 3,4-dihydroxyphenyl lactic acid and Protocatechuic Aldehyde; and c. Determining if pharmaceutical compositions contain the fractions of which position and color are equivalent to the position and the color of 3,4-dihydroxyphenyl lactic acid and Protocatechuic Aldehyde. 